The rate constant for the CO + H2O2 reaction

被引:3
|
作者
Glarborg, Peter [1 ]
Marshall, Paul [2 ,3 ]
机构
[1] Tech Univ Denmark, Dept Chem & Biochem Engn, DK-2800 Lyngby, Denmark
[2] Univ N Texas, Dept Chem, Denton, TX 76203 USA
[3] Univ N Texas, CASCaM, Denton, TX 76203 USA
基金
美国国家科学基金会;
关键词
TRANSITION-STATE THEORY; CARBON-MONOXIDE; HIGH-PRESSURES; SENSITIZED DECOMPOSITION; ELEVATED PRESSURES; KINETIC MECHANISM; HYDROGEN PEROXIDE; COMBUSTION; MIXTURES; IGNITION;
D O I
10.1016/j.cplett.2009.05.028
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The rate constant for the reaction CO + H2O2 -> HOCO + OH (R1) at 713 K is determined based on the batch reactor experiments of Baldwin et al. [ R. R. Baldwin, R. W. Walker, S. J. Webster, Combust. Flame 15 (1970) 167] on decomposition of H2O2 sensitized by CO. The value, k(1) (713 K) = 8.1 x 10(2) cm(3) mol(-1) s(-1), is consistent with spin-unrestricted density functional theory. Extrapolation to a wider temperature range through ab initio calculations yields the rate constant k(1) = 3.6 x 10(4)T(2.5) exp(-14425[K]/T) cm(3) mol(-1) s(-1). The reaction is probably of minor importance in combustion. The present analysis reconciles the batch reactor data of Baldwin et al. with recent high-level theoretical work on the CO + HO2 reaction. (c) 2009 Published by Elsevier B.V.
引用
收藏
页码:40 / 43
页数:4
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